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FDA 510(k)

LSF HA COATED FEMORAL HIP

K-Number: K915617 · 1992-05-28

ApplicantImplant Technology, Inc.
Decision Date1992-05-28
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LSF HA COATED FEMORAL HIP is the device name listed in this FDA 510(k) record. The listed applicant is Implant Technology, Inc.. It received FDA 510(k) clearance on 1992-05-28 under 510(k) number K915617. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LSF HA COATED FEMORAL HIP?

LSF HA COATED FEMORAL HIP is a medical device that received FDA 510(k) clearance on 1992-05-28. The listed applicant is Implant Technology, Inc.. The 510(k) number is K915617.

When did LSF HA COATED FEMORAL HIP receive FDA 510(k) clearance?

LSF HA COATED FEMORAL HIP received FDA 510(k) clearance on 1992-05-28, under 510(k) number K915617.

Who is the listed applicant for LSF HA COATED FEMORAL HIP?

The FDA 510(k) record lists Implant Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LSF HA COATED FEMORAL HIP?

The FDA product code for LSF HA COATED FEMORAL HIP is MEH.

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Other records listing Implant Technology, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K921525HIP JOINT METAL/POLYMER SEMI-CONSTRAINED PROTHESISK920021LSF TOTAL HIP SYSTEM - MULLER-TYPE ACETABULAR CUPK913616LSF DIAGNOSTIC RELATED GROUP CEMENTED HIPK902727LSF CEMENTED FEMORAL HIPK901460LSF(TM) TOTAL HIP SYSTEMK891472IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR

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Related Devices (Code: MEH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261576Icona Hip StemCorin, Ltd.K250375Allure Hip Stem and Intramedullary PlugsWaldemar Link GmbH & Co. KGK251166Mfinity Femoral SystemMedacta International S.A.K251052Trivicta® Hip StemOrtho Development Corp.K242315Resolve Modular Revision Hip StemUnited Orthopedic CorporationK243839Alteon® HA Femoral StemsExactech, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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